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Page 1
A large Calabrian kindred segregating frontotemporal dementia.
Curcio SA, Kawarai T, Paterson AD, Maletta RG, Puccio G, Perri M, Di Natale M, Palermo S, Foncin JF, Hyslop PH, Bruni AC. Curcio SA, et al. J Neurol. 2002 Jul;249(7):911-22. doi: 10.1007/s00415-002-0759-4. J Neurol. 2002. PMID: 12140677
Homozygous carriers of APP A713T mutation in an autosomal dominant Alzheimer disease family.
Conidi ME, Bernardi L, Puccio G, Smirne N, Muraca MG, Curcio SA, Colao R, Piscopo P, Gallo M, Anfossi M, Frangipane F, Clodomiro A, Mirabelli M, Vasso F, Cupidi C, Torchia G, Di Lorenzo R, Mandich P, Confaloni A, Maletta RG, Bruni AC. Conidi ME, et al. Among authors: curcio sa. Neurology. 2015 Jun 2;84(22):2266-73. doi: 10.1212/WNL.0000000000001648. Epub 2015 May 6. Neurology. 2015. PMID: 25948718 Free PMC article.
Heterogeneity within a large kindred with frontotemporal dementia: a novel progranulin mutation.
Bruni AC, Momeni P, Bernardi L, Tomaino C, Frangipane F, Elder J, Kawarai T, Sato C, Pradella S, Wakutani Y, Anfossi M, Gallo M, Geracitano S, Costanzo A, Smirne N, Curcio SA, Mirabelli M, Puccio G, Colao R, Maletta RG, Kertesz A, St George-Hyslop P, Hardy J, Rogaeva E. Bruni AC, et al. Among authors: curcio sa. Neurology. 2007 Jul 10;69(2):140-7. doi: 10.1212/01.wnl.0000265220.64396.b4. Neurology. 2007. PMID: 17620546
Worldwide distribution of PSEN1 Met146Leu mutation: a large variability for a founder mutation.
Bruni AC, Bernardi L, Colao R, Rubino E, Smirne N, Frangipane F, Terni B, Curcio SA, Mirabelli M, Clodomiro A, Di Lorenzo R, Maletta R, Anfossi M, Gallo M, Geracitano S, Tomaino C, Muraca MG, Leotta A, Lio SG, Pinessi L, Rainero I, Sorbi S, Nee L, Milan G, Pappatà S, Postiglione A, Abbamondi N, Forloni G, St George Hyslop P, Rogaeva E, Bugiani O, Giaccone G, Foncin JF, Spillantini MG, Puccio G. Bruni AC, et al. Among authors: curcio sa. Neurology. 2010 Mar 9;74(10):798-806. doi: 10.1212/WNL.0b013e3181d52785. Epub 2010 Feb 17. Neurology. 2010. PMID: 20164095 Free PMC article.
A novel pathogenic PSEN1 mutation in a family with Alzheimer's disease: phenotypical and neuropathological features.
Gallo M, Marcello N, Curcio SA, Colao R, Geracitano S, Bernardi L, Anfossi M, Puccio G, Frangipane F, Clodomiro A, Mirabelli M, Vasso F, Smirne N, Muraca G, Di Lorenzo R, Maletta R, Ghidoni E, Bugiani O, Tagliavini F, Giaccone G, Bruni AC. Gallo M, et al. Among authors: curcio sa. J Alzheimers Dis. 2011;25(3):425-31. doi: 10.3233/JAD-2011-110185. J Alzheimers Dis. 2011. PMID: 21422519
Novel PSEN1 and PGRN mutations in early-onset familial frontotemporal dementia.
Bernardi L, Tomaino C, Anfossi M, Gallo M, Geracitano S, Costanzo A, Colao R, Puccio G, Frangipane F, Curcio SA, Mirabelli M, Smirne N, Iapaolo D, Maletta RG, Bruni AC. Bernardi L, et al. Among authors: curcio sa. Neurobiol Aging. 2009 Nov;30(11):1825-33. doi: 10.1016/j.neurobiolaging.2008.01.005. Epub 2008 Mar 7. Neurobiol Aging. 2009. PMID: 18314228
28 results